IL196132A - Use of an extract of the microalga aphanizomenon flos aquae for the manufacture of a composition for preventing, controlling or treating neurological disease, condition, dysfunction or disorder - Google Patents

Abstract

The invention provides extracts of the microalga Aphanizomenon Flos Aquae Aquae Ralfs ex Born. & Flah. Var. flos aquae (AFA Klamath) and purified components thereof useful for the prevention or treatment of neurological, neurodegenerative and mood conditions or diseases.

Description

Alphanizomenon flos aqua preparation, extracts and purified components thereof for the treatment of neurological, neurodegenerative and mood disorders Nutratee s.r.l.

C. 188493 O 200S/0DU430 PC'J7EP2007/005622 APHAN1ZOMENON FLOS AQUAE PREPARATION, EXTRACTS AND PURIFIED COMPONENTS THEREOF FOR THE TREATMENT OF NEUROLOGICAL, NEURODEGENERATIVE AND MOOD DISORDERS The present invention relates to the microalga Aphanizomenon Flos Aquae Aquae Ralfs ex Born. & Flah. Var. f/os aquae (AFA Klamath). More precisely, the invention provides extracts of AFA Klamath and purified components thereof useful for the prevention or treatment of neurological, neurodegenerative and mood conditions or diseases.

Background of the invention Phenylethylamtne (PEA) is an endogenous amine synthesized by decarboxylation of phenylalanine in dopaminergic neurons of the nigrostriatal system, and may act as a neuromodulator of catecholamine neurotransmission in the brain (1). The most important action of PEA is promoting the neurotransmission of catecholamines. It is known that PEA stimulates the release of acetylcholine as well as dopamine (2). Furthermore PEA increases norepinephrine neurotrasmission (NE) (6) and even serotonin neurotransmission.

Recently it has been shown that PEA can also work as an autonomous neurotransmitter, with its specific neuronal receptors; and that it acts as a true neuromodulator, being also able to depress neurotransmission if needed. (8) From this derive a whole series of effects: stimulation of attention and memory; mood enhancement, with significant antidepressant activity; promotion of empathy and thus sociality, included emotional and sexual behavior; inhibition of hunger; reduction of the need for substance abuse and drug dependency.

The, link hfitwfifin PEA and emotional mood has been confirmed by and so a reduction in the neuromodulation of attention (dopamine) and sedation (serotonine). That is why the drug of choice for ADHD is methylphenidate, a synthetic derivative of PEA, which also acts by stimulating a higher production of PEA (22), and thus of dopamine and norepinephrine, two neurotrasmitters directly involved in the etiology of ADHD.

It is well known the use of amphetamines to control hunger and, consequently, weight. Their use in this area has always been controversial due to their side effects which, given also their tolerance, tend to become potentially very serious over time. This is confirmed by the fact that the main drugs currently used for hunger and weight control are amphetamine-like dopaminergic antidepressants, such as venlafaxine and bupropion. These molecules, as all amphetamines, are synthetic derivatives of PEA. The latter acts as a potent appetite suppressant insofar as its degradation by AO-B enzymes is prevented. onoaminoxidase (MAO) A and B catalyze the degradation of neuroactive and vasoactive amines in the CNS and in peripheral tissues. MAO-B in particular, given its direct and indirect relevance to dopaminergic transmission, is involved in neurological disorders where dopamine is essential, such a depression and mood disorders, Parkinson and Alzheimer diseases. For this reason, MAO-B inhibitors are used in the treatment of such neurological disorders. (26) Description of the invention The invention is based on the identification, in the microatga Aphanizomenon Flos Aquae Aquae Ra!fs ex Born. & Flah. Var. fios aquae (AFA Klamath), of substances that, alone or in combination, exert beneficial effects on various neurological diseases, conditions, dysfunctions or disorders, including neurodegenerative diseases such as Alzheimer's and Parkinson's, multiple sclerosis, hyperactivity and attention deficit disorders (ADHD), autism, depression, memory deficit and mood disturbances. In particular, it has been found that AFA Klamath microalga contains, besides phenylethylamine, which is a neuromodulator characterized by dopaminergic and noradrenergic activity, specific molecules which quite surprisingly proved to be very effective inhibitors of the enzyme monoaminoxidase B (MAO-B), namely: a) the specific AFA-phytochrome; b) the AFA-phycobiliprotein complex containing a phycobilisome formed by C-phycocyanin (C-PC) and phycoerythrocyanin (PEC, including its chromophore phycoviolobilin or PVB) ("AFA-phycocyanins"); c) mycosporine-like amino acids or MAAs. This finding is very important since the PEA contained in the algae, unless protected by MAO-B inhibitors, would be rapidly destroyed upon ingestion by the MAO-B enzyme.

The same molecules that act as MAO-B selective inhibitors, also perform a powerful neuroprotectant role, thus significantly enhancing the ability of the extract to promote neurological health.

Accordingly the invention provides a method for preventing, controlling or treating the above mentioned neurological diseases, conditions, dysfunctions or disorders by administering to a subject in need thereof an AFA Klamath preparation, particularly an extract enriched in such active components, or an isolated and purified component selected from: a) the AFA phytochrome, b) the c-phycocyanin/phycoerithrocyanins complex, as present in AFA or in any other microalgae; c) the mycosporine-like amino acids porphyra and shinorine, as present in AFA or from any other algal source; d) or a mixture thereof.

Preferably the AFA Klamath extract according to the invention is prepared by the following steps: a) freezing the freshly harvested AFA alga and thawing it, or, if the VVO 2U08/(MU430 PC /EI'2U07/0U5622 starting material is dried AFA powder, sonicating the water-diluted AFA powder to disrupt the cells; b) centrifuging the product of step a) to separate the supernatant (retaining most of the cytoplasmatic portion) from the precipitate (retaining most of the cell wall fraction); c) collecting the supernatant containing the water-soluble components.

The resulting product is an extract (indicated as "Basic Extract") which concentrates PEA as well as other synergic molecules such as the AFA phytochrome, the AFA-phycocyanins, and the MAAs. For example, whereas Klamath microalga has a natural content of PEA ranging from 2 to 4 mg/gr, the Basic Extract increases this concentration to a level ranging from 9 to 11 mg/gr (HPLC analysis).

It is possible to further purify the extract by passing it through an ultra-filtration system, preferably through a membrane with a molecular weight cutoff of 30.000 Daltons. The ultra-filtration retentate (Extract A) contains as major active components both the AFA-phycocyanins (mol. weight= 12 .000) and the AFA-phytochrome (mol. Weight 480.000). Interestingly, even though MAAs have a molecular weight well below the cut-off size employed, the retentate also increases the concentration of MAAs.

The Basic Extract obtained by steps a) to c), i.e. without ultra-filtration, is generally preferred as it contains the most appropriate amounts of PEA, AFA-phytochrome, AFA-PC and MAAs. Moreover, this Basic Extract also includes substances such as chlorophyll and carotenes, even though in a reduced proportion, contributing to its antioxidant and anti-inflammatory properties.

In alternative, the active components of AFA Klamath, namely the complex C-phycocyanin/phycoerithrocyanins (C-PC/PEC), AFA phytochrome and MAAs can be isolated and purified, as further described below, and used in a method according to the invention.

In a preferred embodiment, AFA Klamath C-PC/PEC complex, AFA's phytochrome and mycosporine-like amino acids are used as a combined preparation for simultaneous or separate administration to a subject in need thereof; in a yet further preferred embodiment, such a combined preparation contains phenylethylamine as an additional active ingredient. Among the mycosporine-like amino acids, shinorine and porphyra-334 are particularly preferred, as they are contained in relatively higher concentration in AFA Klamath microalgae.

The observed inhibition of monoaminoxidase-B is particularly relevant as it allows to increase dopaminergic transmission and minimize the catabolism of PEA. Significantly, both phytochrome and AFA-phycocyanin inhibit MAO-B in a reversible and mixed way, whereas MAO-B inhibition by MAAs is competitive and reversible; therefore, all three molecules assure high efficacy in physiological conditions and in the absence of side-effects.

In a further aspect, the invention is directed to a nutraceuticat or pharmaceutical composition containing an AFA Klamath preparation, an extract or an isolated component thereof which is preferably selected from the C-PC/PEC complex, as present in AFA or from any other microalgal source, or the isolated C-PC and PEC single components; AFA phytochrome; the mycosporine-like amino acids porphyra and shinorine, as present in AFA algae or from any other algal source; or mixtures thereof; with the optional addition of phenylethylamine. I n a preferred embodiment, the nutritional compositions are dietary supplements in the form of tablets, capsules, beverages; in a further preferred embodiment the pharmaceutical compositions are in the form of tablets, capsules, sachets, syrups, suppositories, vials and ointments and can be used for the prevention or O 2(M8/I)l)(>43() PO7EP2007/005622 7 treatment of neurological or neurodegenerative diseases or conditions indicated above. The AFA Klamath liquid extracts according to the invention can be either used as such or can be dried through methodologies such as freeze-drying, spray-drying or the like. The isolated active components can be formulated using techniques and following procedures that are known to anyone skilled in the art.

The dose of active ingredient will depend on the intended use of the compositions, whether as nutritional supplement or as a pharmaceutical preparation. The effective amount of each component will be generally comprised in the following ranges: PEA= 0.1 -100 mg, preferably 5-30 mg; phytochrome= 0.1 -1000 mg, preferably 0.8-10 mg; MAAs= 0.1-1000 mg, preferably 10-100; phycocyanins= 1-2500 mg, preferably 50-1000 mg.

Detailed description of the invention identification of "AFA-phytochro e", a unique phytochrome typical of Klamath algae Phytochromes are photoreceptors, pigments that plants use to detect light and that are sensitive to light in the red and far-red region of the visible spectrum. They perform many different functions in plants, including the regulation of flowering (through circadian rythms), germination and the synthesys of chlorophyll. The latter is particularly relevant in relation to AFA algae, because the presence of this unique type of phytochrome in AFA may be explained by its lack of the other phycobiliprotein commonly used by other cyanobacteria to complement C-phycocyanin in the process of photosynthesis, namely allo-phycocyanin. While the place of allo-phycocyanin in Klamath algae is taken by phycoerythrocyanin or PEC (see below), it is likely that PEC alone is not sufficient, especially considering that Klamath algae lives in a non-tropical environment which needs a high light harvesting efficiency, and so AFA algae seem to integrate their higher needs with the phytochrorne.

The AFA phytochrorne which has a peculiar structure, is described here for the first time. Over the years, different types of phytochromes have been found in plants, which not only have different phytochrorne genes (3 in rice and 6 in maize, for instance), but in most cases they have significantly different protein components and structure. What makes them all phycochromes is that they all use the same biliprotein, called phytochromobilin, as a light-absorbing chromophore, This chromophore is similar to the phycocyanin's chromophore phycocyanobilin, and is characterized by a single bilin molecule consisting of an open chain of four pyrrole rings (tetrapyrroles). More specifically, in its Pr normal state this biliprotein absorbs light at a maximum of 650-670 nM, whereas when activated by red light it is transformed into Pfr ith an absorbance maximum of 730 nM.

The first cyanobacterial phytochrorne to be discovered, that of Synechocystis, showed to have a weak structural similarity with plant phytochromes. Nevertheless, Synechocystis 's biliprotein is generally considered a phytochrorne insofar as it is a red/far-red reversible chromoprotein. (48) AFA phytochrorne purification and characterization AFA-phytochrome has a biliprotein as its chromophore that absorbs light in the red/far-red spectrum. To establish its structure and activities we have purified the phytochrorne with the following protocol: - Suspend 1 g of extract in 10 ml of 1 K-phosphate buffer, pH 7.0 - Vortex twice for 1 min with half their volume - Incubate cells for 35' with 2% Triton X 100 - Centrifuge at 28000 rpm for 16-18h - Collect supernatant on a sucrose density step gradient - Spin the gradient using swing-out rotors at 150000 g for 12 h - Store at -20°C The phytochrome corresponds to the lysate band of an intense orange color, which is visible at approximately 1 of sucrose, while the phycobilisome stands at approximately 0.75 M. This relation of the two bands also gives a reliable indication about the molecular weight of the phytochrome present in the algae, which is about 4 times that of the trimeric AFA-PC: the latter being 121 Kd, we can preliminarily establish the MW of AFA-phytochrome at approximately 480Kd (Figure 22} Tested for its light-absorbing properties, the phytochrome shows to absorb light with two peaks at 672 nM and 694 nM, which corresponds respectively to Pr (red-light absorbing) e P (far-red light absorbing) forms in a state of equilibrium (Figure 23).

As to the quantity of phytochrome contained in AFA, our first evaluation gives the following preliminary result: 2 mg/gr (or 0.2% DW). As to the extracts, the concentration increases to approximately 0.5% in the Basic Extract, and approx. 1 % in the Extract B. These are low concentrations, yet the antioxidant/antinflammatory potency of this molecule is so strong that even a very small quantity can produce very relevant effects.

Antioxidant activity The purified AFA-phytochrome has shown to be a very powerful antioxidant. I n fact, in absolute terms, the most powerful molecule so far found in Klamath algae. The incubation for 2 hrs. of human plasma samples with oxidative agent CuC at 100 μΜ generates increased levels of malondialdehyde (MDA), a late byproduct of lipid peroxidation which is measured through spectrophotometer at 535 nm after a reaction with thiobarbituric acid (TBA test). When plasma is incubated for 2 hrs at 37°C with CuCl2 100 μΜ together with increasing quantities of AFA-phytochrome (2-16 nM) extracted from AFA algae, a very strong dose-dependent reduction of the MDA levels is observed (Figure 24). In fact, an almost complete inhibition of lipoperoxidation is obtained with MDA levels close to control, with just 16 nM of AFA phytochrome. Significantly, the IC50 of 3.6 nM is 45 times less than that obtained for the PCB. The phytochrome is the main responsible for the antioxidant and neuroprotecting effects of the Basic Extract, which are higher than those of AFA-PC.

Extraction, purification and quantification of MAAs We tested the presence of MAAs in the cyanophyta Aphanizomenon flos-aquae of Klamath Lake, generally known as Klamath algae. To our knowledge, only a very recent report exist on the occurrence of MAAs in any Aphanizomenon species (47); however, such report only identifies porphyra as the MAAs present, whereas our research shows the presence of two MAAs, both porphyra and shinorine. On the other hand, in relation to the overall literature on algae, whereas most of the cyanobacteria reported to date contain shinorine as their primary MAAs, we found a rare occurrence of porphyra-334 as the primary MAA in Aphanizomenon flos-aquae in addition to shinorine. l'oi hyra-j34 XH ΗΟ ¾θϊΤ ¾0ΗCHL S:o2n Sliinorine MAAs were extracted as previously reported. (29) Briefly, 20 mg of AFA powder or 20 mg. of aqueous extract are extracted in 2 ml of 20% (v/v) aqueous methanol (HPLC grade) by incubating in a water bath at 45°C for 2.5 h. After centrifugation (5000 g; GS-15R Centrifuge, Beckman, Palo Alto, USA), the supernatant was evaporated to dryness and re-dissolved in 2 ml 100% methanol, vortexed for 2-3 min and centrifuged at 10000 g for 10 min. The supernatant was evaporated and the extract re-dissolved in the same volume of 0.2% acetic acid for the analysis in HPLC or in 200 μΙ of phosphate buffer (PBS) for the evaluation of antioxidant properties. The samples were filtered through 0.2 μπι pore-sized syringe filters (VWR International, Milan, Italy) before being subjected to HPLC analysis, or to the test of antioxidant properties (see below).

The AAs of Klamath algae have an absorption maximum of 334 nm. Further purification of MAAs was done using a HPLC system (Jasco Corporation, Tokyo, Japan) equipped with a Alltima C18 column and guard (4.6 x 250 mm i.d., 5 μιη packing, Alltech, Milan, Italy), according to the literature (30). The wavelength for detection was 330 nm; the mobile phase was 0.2% acetic acid at a flow-rate of 1.0 ml min-1. Identification of MAAs was done by comparing the absorption spectra and retentions time with standards such as Porphyra and Pterocladia sp., mainly containing porphyra-334, shinorine and palythine, kindly provided by Dr Manfred Klisch, Friedrich-Alexander-Universitat, Eriangen, Germany. Absorption spectra of samples were measured from 200 to 800 nm in a single-beam spectrophotometer (DU 640, Beckman, Palo Alto, USA). The raw spectra were transferred to a computer and treated mathematically for the peak analyses of MAAs.

MAAs were partially purified from AFA sample and from the aqueous extract as described earlier. Extraction of samples with 20% methanol at 45°C for 2.5 h resulted in a prominent peak at 334 nm (MAAs); even if small amounts of photosynthetic pigments (such as phycocyanin at 620 nm) were also extracted with this procedure (see Figure 1 , dashed line). MAA samples were further treated with 00% methanol in order to remove proteins and O 2»08/00043(> PC /EP2007/»»5622 12 salts and finally with 0.2% acetic acid to remove non polar-photosynthetic pigments. The resultant partially purified MAAs had an absorption maximum at 334 nm (Figure 1 , solid line).

Further analysis and purification of MAAs was done by HPLC with a view to find whether the compounds absorbing at 334 nm was a single MAA or a mixture of more than one MAAs. The chromatogram of the sample (Figure 2) shows the presence of two MAAs with retention times of 4.2 (peak 1 ) and 7.6 min (peak 2) that were identified as shinorine and porphyra-334, respectively. Porphyra-334 seems to be the major MAA in AFA since shinorine was present only in small quantities (peak area ratio 1 : 15).

The UV spectra of the purified MAAs confirmed their absorption maximum at 334 nm (Figure 3).

Taking into account that the molar extinction coefficients at 334 nm for shinorine and porphyra-334 are of 44700 and 42300 cm-1 , respectively, we calculated: a) for AFA algae, concentrations of 0.49 mg g- DW for shinorine and 7.09 mg g-1 DW for porphyra-334; the total MAAs content being thus equal to 0.76% algal DW; b) For the Basic Extract, concentrations of 17-21 mg of MAAs (that is 1.7-2.1 % DW).

These are significant data, as the whole AFA contains high constitutive levels of MAAs (0.76% DW), close to the maximal concentration found under UV exposure, i.e. 0,84%. (31 ) Also, we found that the extract has a higher concentration than the whole algae, reaching levels that are much higher than the maximal potential concentration.

MAAs (shinorine and porphyra-334) are structurally simple molecules, with a molecular weight of 300. This allows these water soluble molecules to easily cross the blood-brain barrier, confirming their ability to express their AO-B inhibitory potential in the area where it is mostly needed, the brain. Phycocyanins The phycocyanins are present in the extract at a concentration of 8-10% (for the quantification, see below). Phycocyanins are the blue pigments typical of all cyanobacteria or blue-green algae, although with peculiar characteristics for each specific microalga. (32) As to functional and therapeutic properties of phycocyanins, research has mostly focused so far on those of the microalga Spirulina. The purified phycocyanins from Spirulina have shown to possess antioxidant (33) and anti-inflammatory (34, 35, 36) properties on different physiological systems such as liver (37), respiratory system (38) and brain (39, 40). Such properties of the purified PC from Spirulina can in general be attributed also to the phycocyanins of other algae, given their substantial similarity. Nevertheless, there can exist species-specific differences in the different phycocyanins from different microalgae which can lead to a different potency in the explication of the above described functional and therapeutic properties.

Structural determination and specific characteristics of the Klamath algae's phycobilisomes.

Generally speaking, in the intact cyanobacterial cell phycocyanins (PC) are present inside the phycobilisome in the functional form (αβ)β (41 ). Following the break-up of the cell, the protein can be found in different aggregation states (monomers, dimers, trimers, hexamers) according to the organism analyzed. In the case of Klamath algae, the electrophoretic analysis of the PC, both as contained in the extract and as purified from the extract itself, has shown that the protein is found for the most part in its trimeric form (αβ)3, with a total molecular weight of 121 000. A monomer αβ weighs approximately 40000 (18500 subunit a + 21900 subunit β). The majority of the studies on the purified FC from Spirulina tell us instead that the protein is found in Spirulina in the monomeric form αβ with a molecular weight of approximately 37500, thus showing a different aggregation state relative to the purified PC from AFA.

The chromatographic analysis of the AFA's phycobilosomes has also shown that, as in other cyanobacterial species, the a subunit of PC binds a prosthetic group, while the β subunit binds two. The prosthetic group or chromophore is called phycocyanobilin (PCB) and is responsible both of the blue color of the protein and of its antioxidant power (42).

A fundamental difference between AFA and Spirulina rests on the different structure of the phycobilisome. As opposed to Spirulina, the phycobilisome of AFA Klamath does not contain the pigment allo-phycocyanin, but only the pigment c-phycocyanin bound to a structural component which is missing in Spirulina, namely phycoerythrocyanin (PEC). FEC is a photosynthetic pigment which as of today has been identified only in a limited number of cyanobacterial species (43). PEC has a chemical structure very similar to that of FC, being composed by the two subunits a e β which associate to form monomers and trimers. Nevertheless, while every monomer of PC binds 3 molecules of PCB, PEC possesses the unique characteristic of binding two molecules of PCB to the subunit β and one molecule of phycoviolobilin (PVB) to the a subunit, which is responsible of the purple color of the pigment.

This absolutely is the first time that the phycobilisome of Klamath algae is defined as peculiarly constituted by the union of c-phycocyanin and phycoerithrocyanin, and this different qualitative structure of the phycobilisome of AFA Klamath algae adds a further decisive factor distinguishing AFA from Spirulina.

Figure 4 confirms what has been said, comparing the components of the cellular lysate of AFA with those of another well known cyanobacterium, O 2U08/U00430 1>CT/EI>20 7/005G22 Synechocystis PCC 6803. I n both cyanobacteria it possible to see the blue band representing the phycobilisome, but in AFA algae the phycobilisome presents a lower molecular mass, confirming that, as opposed to common microalgae such as Spirulina, in the AFA phycobilisome only phycocyanins, but not allo-phycocianjns, are present. Furthermore, the Figure shows that in AFA is also present a light purple band (shown by the arrow) which is typical of phycocerythrocyanins, thus proving their presence in the phycobilisome of Klamath algae.

To deepen the definition, each blue band has been further analyzed through HPLC connected to mass spectrometer (RP-HPLC-ESI-MS). Thanks to the different times of retention, the proteins of the phycobilisome have been separated and identified based on their molecular mass. The results obtained are shown in the following tables. First we see that while in Synechocystis (Table 1 ) both phycocyanin (cpcA at 28.2 min and cpcB at 28.9 min) and allo-phycocyanin (apcA at 30.7 min and apcB at 31 .2 min), in AFA (Table 2) only phycocyanin (cpcA at 28.8 min and cpcB at 30.0 min) is present. Secondly, in AFA a protein with molecular mass of 19469 has been identified which is not present in Synechocystis and which corresponds to the beta subunit of the phycoerythrocyanin with two bitins attached (pecB a 25.0 min).

TABLE 1: proteins present in the phycobilisome of Synechocystis. (continue) VVO 2008/000430 PCT/fc÷P2!)07/0U5622 16 TABLE 2: proteins present in the phycobilisome ofAFA Klamath algae (continue) WO 20118/(10043(1 ΡθνΕΙ^ΙΚΠ/ΟΟδδΖΖ 17 This unique structure is an important element to explain the stronger antioxidant and anttnflammatory action of the whole AFA-PC relative to its PCB. Antioxidant and antinflammatory properties become relevant in this context insofar as they generate a strong neuroprotection; the whole PC is more powerful than its PCB also in terms of neuroprotection, which clearly indicates that the other active component besides PCB in the phycobilisome, namely PEC with its specific PVB chromophore, is very likely the most active health-enhancing principle in AFA-PC. That the purified AFA-PC does indeed contain not only the C-PC with its PCB chromophore, but also PEC and its PVB chromophore is evident by looking at the spectrometry of the extract resulting from the purification (Figure 5). In fact, the absorption maximum of C-PC is 620 nm, which in the spectrometry of Figure 5 represents the top of the peak. But the absorption maximum of PEC is known to be 566 nm for the a-subunit (phycoviolobilin or PVB) and respectively 593 nm and 639 nm for the two PCBs of the β-subunit. All three values are indeed included in the bell-shaped peak constituting the spectrometric profile of the purified PC. In consideration of the strong link, very difficult to break, between C-PC and PEC in AFA algae, this confirms that besides the C-PC, also the PEC is necessarily part of the purified PC extract. This in turn means that the PC from AFA is significantly different, both structurally and functionally, from the PCs of other cyanobacteria, including the one from Spirulina, on which most studies have been done; and that this difference consists in having only one part in common, namely C-PC, but not the other; with the consequence that, while the properties of C-PC can also be attributed to the C-PC component of the AFA-PC, the properties of the whole PC from AFA, in its being a C-PC/PEC complex (including its chromophores PCB and PVB), are exclusively attributable to it (as well as to any C-PC/PEC complex present in any other microalgae).

Purification methodologies (Figure 5) PC was purified from the dried AFA extract as follows: suspend 500 mg of extract in 50 ml of 100 m Na-phosphate buffer pH 7.4; centrifuge at 2500 rpm for 10' at 4°C; gather the supernatant and add solid ammonium sulfate to a 50% saturation; precipitate the proteins for 60 min at 4°C while keeping the sample in agitation; centrifuge at 10,000 rpm for 30 min at 4°C; discard the clear colourless supernatant and resuspend the blue precipitate in a small volume of 5 mM Na-phosphate buffer pH 7.4; dialyse overnight at 4°C against the same buffer; place the dialysed PC in a hydroxyapatite column balanced with 5 mM Na-phosphate buffer pH 7.4; elute the sample with Na-phosphate buffer pH 7.0 of increasing ionic strength (from 5 to 150 mM); gather the fractions and read the absorbance at 620 nm and 280 nm with the spectrophotometer; pool the fractions in which Abse2o AbS28o > 4 (index of pure PC); precipitate the PC with ammonium sulfate at 50% saturation for 1 hour at 4°; centrifuge at 10,000 rpm for 30' at 4°C; discard the supernatant and suspend again the PC in a 150 mMof Na-phosphate buffer Ph 7.4; dialyse against the same buffer at 4°C; transfer the purified PC in a flask and store in darkness at +4°C or -20°C.

Quantification of phycocianin To measure the molar concentration of pure PC we used its coefficient of molar estinction ε at 620 nm, which for the trimeric form (αβ)3 is equal to 770000 M-1 cm-1. This means that a solution of 1 M of PC at 620 nm has an absorption value of 770000.

To measure the concentration of PC in the extract we use the coefficient of specific extinction E % at 620 nm of 70 I g-1 cm-1. This means that a solution containing 1 % of PC (that is 1 g/100 ml) at 620 nm absorbs 70. Based on these calculations, the average content of PC in the extract is equal to 80-100 mg/g DW (8-10% DW).

Purification of the PCB chromophore (Figure 6) • Suspend 500 mg of extract in 50 ml of distilled H2O.

• Centrifuge at 2500 rpm for 10' at 4°C.

· Decant the deep blue supernatant and precipitate the PC with trichloroacetic acid at 1 %.

• Incubate for 1 h in the dark at 4°C, while agitating.

• Centrifuge at 10000 rpm for 30' at 4°C.

• Gather the pellet containing PC and wash 3 times with methanol. · Re-suspend the pellet in 10 ml of methanol containing 1 mg/ml of HgCI2.

• Incubate for 20 h at 42°C in darkness to release the PCB from PC.

• Centrifuge at 2500 rpm for 10" to remove the proteins.

• Add to the supernatant containing PCB β-mercaptoethanol (1 μΙ/ml) to precipitate the HgCI2.

• Incubate at -20°C for 24 h.

• Centrifuge at 10000 rpm for 30' at 4°C to remove the white precipitate.

O 2(K)8/()()()43() PCT/EP2007/005622 21 ■ Add to the supernatant 10 ml of methylene chloride/butanol (2:1 , v/v).

. Wash with 20 ml of distilled H20 and centrifuge at 3000 rpm for 10'.

• Remove the upper phase, harvest the lower part containing PCB. · Wash the PCB in 15 ml H20 3 times.

• Dry under nitrogen and store at -20°C.

EVALUA TION OF THE MAO-B INHIBITION BY AFA KLAMA TH EXTRACT AND BY ITS CONSTITUTIVE ACTIVE PRINCIPLES PHYTOCHROME, PHYCOCYANIN AND MAAs We have tested the MAO-B inhibitory activity of the Basic Extract using the specific substrate benzylamine (1 mM). The test was performed by a spectrophotometer at 30°C with a wavelength of 250 nm, by pre-incubating MAO-B (2 pg/ml) with different concentrations of the water-soluble and lipid-soluble components of the basic extract, as produced by the steps a) to c) described above (initial concentration 10 mg/ml). The water-soluble component-enriched extract has been prepared by re-suspending the aqueous extract in water and collecting the supernatant after centrifugation. The lipophilic component-enriched soluble extract has been obtained by re-suspending the extract in acetone; afterwards the supernatant has been dried, and the pellet has been re-suspended in DMSO, a solvent compatible with the dosage of MAO-B.

As shown in Figure 7A, the water-soluble fraction inhibits MAO-B in a dose-dependent manner, while the lipophilic fraction does not inhibit the enzyme. The water-soluble fraction of the AFA Basic Extract is a potent selective MAO-B inhibitor, with an IC50 of 6.9 pL. Its MAO-B selectivity is 4 (ICso MAO-B/ IC50 MAO-A > 4,05) (Figure 7B).

The Lineweaver-Burk plot in Figure 8 shows that such inhibition is reversible and of a mixed type in relation to competition, with a decrease in the Vmax and increase of the Michaelis-Menten Km constant. Plotting the slope vs. the concentration of the hydrosoluble fraction of the AFA extract, a 1 pl_ inhibition constant Ki, is obtained. Compared to the hydrosoluble fraction of the Basic Extract, this low K, value indicates a high affinity for the AO-B enzyme.

The fact that the extract's inhibition is reversible means that it performs a physiological activity plausibly devoid of side effects. As to the mixed competition, it is very likely due to the complex nature of the extract, including different functional molecules, some competitive and others non-competitive. The main active components of the extract are the AFA-phytochrome (0,5% DW); phycocyanins (8-10% DW); and the MAAs or mycosporine-like aminoacids (1 .7-2.1 % DW), which we have tested individually as MAO-B inhibitors.

MAO-B inhibition by phycocyanins The test has been done through a spectrophotometer at 30°C with a wavelength of 250 nm, using benzylamine as a substrate, by preincubating MAO-B with various concentrations of purified PC from AFA (0.5-4 μΜ). As shown in Figure 9, AFA-PC causes a dose-dependent decrease of MAO-B activity, with an IC50 of 1 ,44 μΜ. The MAO-B selectivity of AFA-PC is higher than 3.5 (IC50MAO-B/IC50MAO-A > 3.5).

The Lineweaver-Burk plot in Figure 10 shows that, as with the extract, the inhibition is reversible and of a mixed type (competitive and non-competitive) with modification of both Vmax and Km.

By plotting the slope vs. the PC concentration we obtain the value of the inhibition constant Ki, which here is of 1 .06 μΜ. The inhibition constant measures the affinity of the inhibitor for the enzyme: a high Kj indicates a low affinity for the enzyme and viceversa. In this instance, the low Ki value indicates a high affinity of AFA PC towards MAO-B.

O 20UH/000430 l,CT/El,2(K)7/0<)5622 23 MAO-B inhibition by MAAs The activity of AO-B on a benzylarnine substrate has been evaluated in relation to increasing concentrations of MAAs (0.5-8 μΜ), previously purified from the Basic Extract with 20% methanol. Figure 1 1 shows the dose-dependent MAO-B inhibition by MAAs, with an IC50 of 1 .98 μΜ. The MAO-B selectivity of MAAs is higher than 2 (ICsoMAO-B/lCsoMAO-A >2,02).

The Lineweaver-Burk plot (Figure 12) shows that the inhibition is both reversible and competitive, with an increase of Km but no variation of the Vmax. This means that MAAs, thanks to their chemical structure, compete with the substrate for the link to the active site of the enzyme. Plotting the slope vs. the concentration of MAAs (Figure 13) we obtain the value of the inhibition constant Κ,·, which is of 0.585 μΜ, which demonstrates a very high degree of affinity for the enzyme.

MAO-B inhibition by AFA phytochrome The test has been done through a spectrophotometer at 30°C with a wavelength of 250 nm, using benzylarnine as a substrate, by preincubating MAO-B with various concentrations of purified AFA phytochrome (8.3 - 66.4 nM). As shown in Figure 15, AFA phytochrome causes a dose-dependent decrease of MAO-B activity, with an ICso as low as 20.2 nM.

The Lineweaver-Burk plot in Figure 16 shows that, as with the extract, the inhibition is reversible of a mixed type (competitive and non-competitive) with modification of both Vmax and Km.

By plotting the slope vs. the AFA phytochrome concentration we obtain the value of the inhibition constant Ki, which here is of 10.48 nM. The inhibition constant measures the affinity of the inhibitor for the enzyme: a high Ki indicates a low affinity for the enzyme and viceversa. In this instance, the extremely low K, value indicates a very high affinity of AFA phytochrome towards MAO-B.

WO 20U8/0 Even more than MAAs, the phytochrome has proven to be the most powerful MAO B inhibitor of all known substances to date. Its very high affinity for the MAO-B enzyme, and its effective inhibition at dosages of few nanomolars, make this molecule not only a perfect therapeutic agent on its own, but the factor that seems to provide the most important contribution to the high neurological effectiveness of the AFA extract(s).

It should be added that some of the considerations relating to the MAAs and phythcrome can also be applied to the in vivo behaviour of phycocyanins. We know that PC generate neuroprotective effects on the brain in vivo, and so that they are able to cross the blood-brain barrier. (44) This means that they are also able to realize in vivo their MAO-B inhibitory activity in the brain. The molecular weight of the chromophore is indeed only 700, that is not much more than the molecular weight of the MAAs. The same holds true for the chromophore of the phytochrome, the phytochromobilin, structurally similar to phycocyanobilin.

In conclusion, the activity of MAO-B inhibition on the part of the extract and its active components, AFA phytochrome, AFA-PC and MAAs, is extremely relevant, as both the molecules and the extract place themselves at the highest level of activity, equal or higher than the pharmacological substances, and greatly superior to any natural molecule tested, as shown in the following table (45): Table 3: Comparative kinetics parameters (ICso e Ki) of MAO B inhibition from known synthetic and natural inhibitors.

AO-B Inhibitors IC50 Ki Inhibition type Deprenyl 0.31 μ 0.002 μΜ Irreversible Epicatechine 58.9 μΜ 21 μΜ Mixed Catechine 88.6 μΜ 74 μ Mixed Non Harman alkaloid 6.47 μΜ 1.12 μΜ Mixed Piperine 91 .3 μΜ 79.9 μΜ Competitive Paeonol 42.5 μΜ 38.2 μΜ Competitive Emodin 35.4 μΜ 15.1 μΜ Mixed AFA phycocyanin 1.44 μΜ 1.06 μΜ Mixed AFA MAAs 1.98 μΜ 0.585 μΜ Competitive AFA phytochrome 0.02 μΜ 0.010 μΜ Mixed As shown by the table, only phycocyanins and MAAs have an 1C50 slightly higher than 1 μΜ, thus very close to that of Deprenyl (0.31 μΜ), and tens of times lower than the IC50 of the other molecules considered. AFA phytochrome, on the other hand, has an IC50 15 times lower than that of Deprenyl. The same is true for the inhibition constant Ki which measures the affinity of the inhibitor for the enzyme. AFA-phycocyanins have a K of around 1 μΜ, like the non Harman alkaloids of coffee and tobacco (but of course without any of the problems associated with those two substances). On the other hand, MAAs and the AFA phytochrome are the only molecules, together with Deprenyl, to have a Ki lower than 1 μΜ, and so a very high affinity for the MAO-B. In fact, AFA phytochrome is the only natural molecule, besides selegyline/Deprenyl, whose Kj is in the order of a few nanomolars. And yet, there is an essential difference between selegiline/Deprenyl and the molecules of the AFA extract: the former is an irreversible inhibitor, thus characterized by potential side effects; whereas AFA Klamath MAO B inhibiting molecules are all reversible, characterized by a physiological activity devoid of the problems associated with synthetic molecules.

Figure 14 shows graphically the MAO-B inhibitory activity of the three molecules of AFA in relation to Deprenyl. Given the synergy of all three molecules in the Basic Extract (and other AFA extracts), the overall MAO-B inhititory activity of the Basic Extract results very high. Something that becomes particularly relevant considering also the high quantity of PEA present in it. If we compare the basic extract with deprenyl on the base of its PC content, we obtain that the Basic Extract reaches the IC50 at a PC dosage as low as 0,05 μΜ, which would indicate a potency 7.5 times higher than Deprenyl (and tens of times higher than the natural substances). This makes sense in light of the potency of the phytochrome contained in the Basic Extract: in fact 7.5 times is an average between the inhibitory potency of PC and MAAs, which is slightly lower than Deprenyl, and that of the phytochrome, which is 15 times higher (Figure 1 ). This also shows that the higher potency of the extract relative to the purified AFA-PC is for the most part due to the phytochrome.

Moreover, the extract still maintains the advantage of being a natural substance acting physiologically, whose MAO-B inhibition is reversible and mainly competitive, thus devoid of the side effects potentially associated with irreversible molecules such as Deprenyl and other synthetic substances. (46) The further advantage of the extract is its high content of phenylethylamine, a powerful dopaminergic neuromodulator which works in total synergy with other molecules, a synergic activity that we can thus summarize: - Phenylethylamine or PEA has twofold dopaminergic activity, both as it stimulates the release of dopamine from the nigrostriatal tissue, and as it inhibits the post-synaptic reuptake of dopamine itself; - Phytochrome, MAAs and phycocyanins, as powerful MAO-B inhibitors, also increase dopaminergic transmission insofar as a reduced activity MAO-B implies a longer life of neuroamines, including dopamine; - Phytochrome, MAAs and phycocyanins, as MAO-B inhibitors, also prolong the life and activity of phenylethylamine, which is itself the object of the deamination activity of the MAO-B enzyme, with the consequent creation of a virtuous circle of further support to dopaminergic transmission and activity and to the more genera! neuromodulation produced by PEA.

- Finally, the powerful antioxidant and anti-inflammatory activity of phycocyanins, together with their or their chromophore ability to cross the blood-brain barrier; as well as the extremely high antioxidant activity of the phytochrome and the less strong yet significant antioxidant activity of MAAs, generates a neuroprotection that shields the different active molecules and more generally the neurological virtuous cycle they create, from any oxidative and inflammatory damage.

NEUROPROTECTION We have tested the neuroprotectant properties of the AFA extract, the specific AFA-PC and its chromophore PCB, as well as MAA's against the neurotoxic effect of glutamate.

Glutamate is the main excitatory neurotransmitter in the mammalian central nervous system, but over-stimulation of its NMDA subtype receptor in neurons triggers a massive intracellular accumulation of Ca2+, leading to cell death. In addition intramitochondrial Ca2+ accumulation, after NMDA receptor stimulation, transient increases in free cytosolic Ca2+ activate the neuronal isoform of nitric oxide synthase (NOS) (49), an enzyme that forms nitric oxide (NO ) or, mainly in primary neurons, its superoxide (02 -) reaction product, peroxynitrite (ONOO-).

The exposure of neurons to glutamate was carried according to a slightly modified method (50): culture medium was removed and neurons were washed once with prewarmed 37°C buffered Hanks' solution (5.26 mM KCI, 0.43 m ΚΗ2Η2Ρθ4, 132.4 mM NaCI, 4.09 mM NaHC03, 0.33 mM NaaHPO^ 20 mM glucose, 2 mM CaCI2, and 20 mM HEPES, pH 7.4) and pre-incubated in the absence or presence of several concentrations of AFA extract (1 -50 nM), PC (10-1000 nM), PCB (10-1000 nM) and MAA (1 -10 μΜ) in prewarmed 37°C buffered Hanks' solution. After 30 min of pre-incubation, L-glutamate was added from concentrated solutions to the final concentration indicated 100 μΜ plus 10 μΜ glycine. Neurons were incubated at 37°C for 15 min, the buffer was aspirated, replaced with DMEM and the cells were incubated at 37°C for further 24 h in the absence of effectors.

Apoptosis was assessed by staining the nuclei of cells with DAPl (50), a membrane-permeable fluorescent dye that binds DNA and allows quantification of apoptotic neurons, i.e. , neurons displaying fragmented or condensed nuclei. Briefly, 24 h after glutamate exposure, neuronal cultures were washed with warm PBS (37°C) and fixed with 4% (wt/vol) paraformaldehyde in PBS for 30 min at room temperature. After being washed with PBS, cells were exposed to 3 μΜ DAPl for 10 min at room temperature in the dark and were then washed twice with PBS. Cells were scored for chromatin condensation by fluorescence microscopy, using a fluorescein filter (330-380 excitation; 30X magnification). Total and apoptotic nuclei were counted. In all cases, approximately 600-1 ,000 cells were O 2008/00043(1 l'CT/El>2U07/005f>22 29 counted per well by an operator blind to the protocol design. Measurements from individual cultures were performed in duplicate and results are expressed as the mean S.E.M . values for the number of culture preparations indicated. Statistical analysis of the results was determined by Kruskal-Wallis test followed by the least significant difference multiple range test. In all cases, p-0.05 was considered significant.

Through this gluatamate damage test we have shown for the first time the neuroprotective ability of AFA Basic Extract, AFA-PC, its PCB and MAAs. As shown by Figure 1 8, the addition of glutamate to the cultured neuron cells has increased the level of apoptosis to a percentage of 22,9% ± 3 n = 4 (p< 0.05); while the simultaneous addition of the AFA Basic Extract has generated a very high protection against glutamate toxicity, lowering the level of apoptosis below the control level of (6.3% ± 1 p> 0.05) already with as low an amount of extract as 1 nM (results are means ± SEM from 3 to 8 different cell cultures. # Significantly different when compared with control group (p<0.05); * Significantly different when compared with the glutamate control (p<0.05). As to the protection afforded by MAAs, they also lower the level of apoptosis below the control level, with the higher dosage of 1 μ (Figure 19) results are means ± SEM from 3 to 8 different cell cultures. # Significantly different when compared with control group (p<0.05); * Significantly different when compared with the glutamate control (p<0.05).). Regarding AFA-PC and PCB, we see that their inhibition of apoptosis is very similar: their addition to the cell culture lowers the degree of apoptosis below the control with a dosage of approximately 10 nM (Figures 20 and 21 - results are means ± SEM from 3 to 8 different cell cultures. # Significantly different when compared with control group (p<0.05); * Significantly different when compared with the glutamate control (p<0.05)).

The degree of inhibition of AFA-PC is approximately equal to that of O 2008/000430 l,C'tVEP2007/005622 PCB. This is somewhat surprising, given that the PCB, supposedly its most active principle, once purified and thus more concentrated, should be significantly stronger than the whole molecule of which is the active component. The fact that it has practically the same potency means that in the whole PC there are other factors that may actually be even more potent than the PCB itself. We know that the whole PC is composed, besides C-PC and its PCB chromophore, of PEC, which includes as its chromophores both PCB and PVB (phycoviolobilin). Therefore, we can here assume that the factor that create a significant difference in potency between the purified PCB and the whole PC is precsiely the PEC component, particularly its PVB chromomphore, which is assumed to be a very strong antioxidant.

In terms of neuroprotection, MAAs seem to play a role, but significantly less than PC and PCB. However, the most powerful neuroprotectant is clearly the whole AFA extract, which is able to completely inhibit cell apoptosis at just 1 nM (nanomolar). This is 10 times the potency of PC and PCB. This can certainly be explained with the synergy of many different antioxidant factors present in the whole AFA extract; yet, since we have seen above that the AFA-phytochrome is possibly the most powerful antixidant to date, being able to almost completely inhibit MDA (a late by-product of lipid-peroxidation) formation with just 16 nanomolars, it is very likely that AFA-phytochrome is the more important factor in explaining the higher potency of the Basic Extract. We can thus conclude that AFA-phytochrome, as well as any and all phytochromes, are important neuroprotective agents.

BIBLIOGRAPHY 1 . Zhou G. et al., Platelet monoamine oxidase B and plasma β-phenylethytamine in Parkinson's disease, in J Neurol Neurosurg Psychiatry, 2001 ; 70:229-231 , 229. 2. Ispida K. et al., β-phenylethylamine stimulates striatal acetylcoline re/ease through activation of the AMPA glutamatergic pathway, in Biol Pharm Bull 2005 Sep.; 28(9): 1626-9. 3. Barroso N. , Rodriguez ., Action of β-phenylethylamine and related amines on nigrostriatal dopamine neurotransmission, in European Journal of Pharmacology, 297 (1996), 195-203, 200. 4. Dyck L. E., Release of monoamines from striatal slices by phenelzine and β-pheny/ethy/amine, in Prog Neuropsychopharmacol Biol Psychiatry, 1983, 7:797-800; Philips S.R. , Robson A.M., In vivo release of endogenous dopamine from rat caudate nucleus by phenylethylamine, in Neuropharmacology 1983, 22: 1297-1301 ; Raitieri m., et al. , Effect of sympathomimetic amines on the synaptosomal transport of noradrenaline, dopamine and 5-hydroxytryptamine, in Eur J Pharmacol 977, 41 :133-143.

. Janssen P.A.J, et al., Does phenylethylamine act as an endogenous amphetamine in some patients?, in International Journal of Neuropsychopharmacology 1999 , 2: 229-240, 232. 6. Paterson I. A. et al., 2-phenylethylamine: a modulator of catecholamine transmission in the mammalian central nervous system?, in Journal of Neurochemistry (1990), 55:1827-1837. 7. Sabelli H.C., Javaid I. J ., Phenylethylamine Modulation of Affect: Therapeutic and Diagnostic Implications, in Journal of Neuropsychiatry (1995), 7(1 ):6-14, 7. 2, Mauro Federici et al., Trace Amines Depress Gabab Response In Dopaminergic Neurons By Inhibiting Cirk Channels, in Molecular Pharmacology Fast Forward. Published on January 1 1 , 2005 as doi: 10.1 124/mol.1 04.007427. 9. Gusovsky F. et al., A high pressare liquid chromatography method for plasma phenylacetic acid, a putative marker for depressive disorders, in Anal Biochem, 1985 Feb. 15; 145(1 ): 101 -5. In this study, the depressed patients had a PAA level in the plasma of 327.64 +/- 45.44 ng/ml, against the 536.18 +/- 54.99 ng/ml. of the control group. In another study, in the urine of the depressed patients was found and average PAA of 66 +/- 23 mg/die, against the 104 +/- 23 mg/die of non depressed patients. See Sabelli HC. et al., Urinary phenylacetic acid in panic disorder with and without depression, in Acta Psychiatr Scand 1990 Jul;82(1 ):14-6.

. Szabo A. et al., Phenylethylamine, a possible link to the antidepressant effects of exercise ?, in Br J Sports Med 2001 Oct; 35(5):342-3. 1 1 . Sabelli H et al., Sustained antidepressant effect of PEA replacement, in J Neuropsychiatry Clin Neurosci, 8(2): 168-71. 12. Miura Y., Plasma beta-phenytethylamine in Parkinson's disease, in Kurume Med J 2000;47(4):267-72. 13. Ibid., 14. Ebadi M. et al., Neuroprotective actions of selegiline, in J Neurosci Res 2002 Feb 1 ;67(3):285-289.

. Kemppainen N. et al. , Different pattern of reduction of striatal dopamine reuptake sites in Alzheimer's disease and ageing, in J Neural Transm 2001 ; 108(7):827-36. 16. Knoll J. , (-)Deprenyl (Selegiline): past, present and future, in Neurobiology (Bp) 2000;8(2):179-99. 17. Knoll J., The pharmacological basis of the beneficial effects of WO 20US/000430 PCT/lil,2 . Citazione solo di Benedetti et al. LifeScience; o menzione del parallelo brevetto? Attendere I'anno provisional in attesa di effettuare studi sulla neuroprotezione? 21. Kusaga A., Decreased beta-phenylethylamine in urine of children with attention deficit hyperactivity disorder and autistic disorder, in No To Hattatsu 2002 May; 34(3):243-8; atsuishi T, Yamashita Y., Neurochemical and neurotransmitter studies in patients with learning disabilities, in No To Hattatsu 1999 May;31 {3):245-8. 22. Kusaga A. et al. , Increased urine phenylethylamine after methylphenidate treatment in children with ADHD, in Ann Neurol 2002 Sep;52(3):372-4. 23. Jain AK,. Et al. , Bupropion SR vs. placebo for weight loss in obese patients with depressive symptoms, in Obes Res. 2002 Oct; 0(10): 1049-56. 24. Rudol h et al., A randomized, placebo-controlled, dose-response trial of venlafaxine hydrochloride in the treatment of major depression, in J Clin O 2008/000430 PdVEP20U7/005fi22 34 Psychiatry (1998); 59(3):1 16-22.

. PEA is a lipid-soluble molecule quite subject to be damaged by heat. This means that drying methods using high temperatures, such a freeze drying, usually have lower concentration of PEA. The highest content of PEA is found in the algae dried with the Refractance Window® method. It is from this type of algae that the Basic Extract is realized. 26. Yamada . et al., Clinical Pharmacology of MAO Inhibitors: Safety and Future, in Neurotoxicology 2004; 25:215-21 ; Youdim ., et al., Therapeutic Applications of Selective and Non-Selective Inhibitors of Monoamine Oxidase A and B that do not Cause Significant Tyramine Potentiation, in Neurotoxicology 2004;25:243-50. 27. Groniger A et al., Photoprotective compounds in cyanobacteria, phytoplankton and macroalgae-a database, in J Photochem Photobiol B. 2000 Nov;58(2-3):115-22. 28. Suh HJ et al., Mycosporine glycine protects biological systems against photodynamic damage by quenching singlet oxygen with a high efficiency, in Photochem Photobiol. 2003 Aug;78(2): 109-13. 29. Groniger A et al., Photoprotective compounds in cyanobacteria, phytoplankton and macroalgae-a database, in J Photochem Photobiol B. 2000 Nov;58(2-3): 1 15-22.

. Sinha RP et al., induction of mycosporine-like amino acids (MAAs) in cyanobacteria by solar ultraviolet-B radiation, in J Photochem Photobiol B. 2001 Jul; 60(2-3):129-35. 31 . Garcia-Pichel F et al., Occurrence of UV- Absorbing, Mycosporine-Like Compounds among Cyanobacterial Isolates and an Estimate of Their Screening Capacity, in Appl Environ Microbiol. 1993 Jan;59(1 ):163-169. 32. Glazer A.N. , Phycobiliproteins, in Methods Enzymol, 1988, 167: 291-303.

O 21)08/01)0430 PCT/KI*20l»7/005622 33. Bhat V.B., et al. , C-phycocyanin: a potent peroxyl radical scavenger in vivo and in vitro, in Biochem Biophys Res Commun., 2000; 275(1 ):20-25; Romay, C. et al., Antioxidant and antinflammatory properties of C-phycocyanin from blue-green algae, in Inflam Res, 1998, Jan.; 47(1 ): 36-41 . 34. Reddy CM., et al. , Selective Inhibition of cyclooxygenase-2 by C-phycocyanin, in Biochem Biophys Res Commun. 2000; 277(3): 599-603.

. Gonzales R. , et al., Anti-infl ammatory activity of phycocyanin extract in acetic acid induced colitis in rats, in Pharmacol Res, 1999; 39(1 ): 55-9. 36. Gonzales R., et a I., Anti-infl ammatory activity of phycocyanin extract in acetic acid induced colitis in rats, in Pharmacol Res, 1999; 39(1 ): 55-9. 37. Vadiraja BB. et al. , Hepatoprotective effect of C-phycocyanin:protection for carbon tetrachloride and R-(-f-)-pulegone-mediated hepatotoxicty in rats, in Biochem Biophys Res Commun, 1998; 249(2):428-31. 38. Romay C, et al., Phycocyanin extract reduces leukotriene B4 levels in arachidonic induced mouse-ear infl ammation test, in J Pharm Pharmacol. 1999,51 (5):641 -42. Come e noto, il leucotriene B4 e uno dei fattori principalmente responsabili di patologie respiratorie quali asma e allergie. 39. Rimbau V., et al., Protective effects of C-phycocyanin against kainic acid-induced neuronal damage in rat hippocampus, in Neurosci Lett 1999, 276(2):75-8. 40. Rimbau V. et al., C-phycocyanin protects cerebellar granule cells from low potassium/serum deprivation-induced apoptosis, in Naunyn Schmiedebergs Arch Pharmacol '2001 ; 364(2): 96-104. 41. Glazer A.N., Phycobilisomes, in Methods Enzymon 98Q, 167;304-312. 42. Htrata T., et al., Antioxidant avtivities of phycocyanobilin prepared from Spirulina latensis, i n J Appl Phycol 2000, 12:435-439. 43. Fuglistaller P. , et al., Isolation and characterization of phycoerythrocyanin and chromatic adptation of the thermophilic cyanobacterium Mastigocladus laminosus, in Arch Microbiol 1981 , 129:268-274. 4 . Rimbau V., et al., Protective effects of C-phycocyanin against kainic acid-induced neuronal damage in rat hippocampus, in Neurosci Lett 1999, 276(2):75-8. 45. The data in this table are drawn from the following studies: Magyar K. et al., Pharmacological aspects of (-)-deprenyl, in CurrMed Chem, 2004 Aug, 11 (15):2017-31 ; Hou et al., Monoamine oxidase B (MAO-B) inhibition by active principles from Uncaria rhyncophylla, in Journal of Ethnopharmacology 100 (2005) 216-220; Herraiz T, Chaparro C, Human monoamine oxidase is inhibited by tobacco smoke: β-carboline alkaloids act as potent and revesible inhibitors, in Biochemical and Biophysical Research Communications 326 (2005) 378-386; Kong LD et al., Inihibition MAO-A and B by some plant-derived alkaloids, phenols and anthraquinones, in Journal of Ethnopharmacology ' 91 (2004) 351-355. 46. Yoshida S. et al., Fluorinated phenylcyclopropylamines. Part 3: Inhibition of monoamine oxidase A and B, in Bioorganic & Medicinal Chemistry 12 (2004) 2645-2652. 47. Torres A. et al., Porphyra-334, a potential natural source for UVA protective sunscreens, in Photochem. Photobiof. Sci. 5 (2006) 432-435. 48. Hughes J, Lamparter T., Prokaryotes and Phytochrome. The Connection to Chromophores and Signaling, in Plant Physiology, December 1999, Vol. 121 , pp. 1 059-1068. 49. Garthwaite et al., Endothelium-derived relaxing factor release on activation ofNMDA receptors suggests role as intercellular messenger in the brain, in Nature. 1988 Nov 24;336(6197):385-8. 50. Delgado-Esteban M. et al., D-Glucose prevents glutathione oxidation and mitochondrial damage after glutamate receptor stimulation in rat cortical primary neurone, in J Neurochem. 2000 Oct;75(4): 1618-24.

Claims (13)

1. The use of i) an extract of the microalga Aphanizomenon Flos Aquae Aquae Ralfs ex Born. & Flah. Var. flos aquae (AFA Klamath), wherein the extract is prepared by the following steps: 5 a) freezing the freshly harvested AFA alga and thawing it, or, if the starting material is dried AFA powder, sonicating the water-diluted AFA powder to disrupt the cells; b) centrifuging the product of step a) to separate the supernatant from the precipitate; 10 c) collecting the supernatant containing the water-soluble components, ii) an isolated component of the microalga Aphanizomenon Flos Aquae Aquae Ralfs ex Born. & Flah. Var. flos aquae (AFA Klamath) which is selected from C-Phycocyanin/phycoerithrocyanins complex (C-PC/PEC), their separate chromophores phycocyanobi!in (PCB) and phycoviolobilin (PVB), the 15 AFA-phytochrome and mycosporine-like amino acids (MAAs), or a mixture thereof, for the manufacture of a composition for preventing, controlling or treating a neurological disease, condition, dysfunction or disorder.

2. The use according to claim 1 , wherein said neurological disease, condition, 20 dysfunction or disorder is one of the following: Alzheimer disease, Parkinson diseases, multiple sclerosis, hyperactivity and attention deficit disorders (ADHD), autism, depression, memory deficit and mood disturbances.

3. The use according to claim 2, wherein the AFA Klamath extract is further purified by subjecting said supernatant to ultra-filtration using an ultrafiltration 25 membrane with molecular weight cut-off of 30,000 Daltons. AMENDED SHEET -04-2008 . EP2007005622 - 39 -

4. The use according to claim 1 , wherein the isolated component is a mycosporine-like amino acid selected from shinorine and porphyra-334. Porp yra-3.>4 Stiinoi ine

5. 5. The use according to claim 1 , wherein the isolated component is the phycocyanin/phycoerithrocyanin complex (C-PC/PEC) or a single sub-component thereof, namely C-PC or PEC.

6. The use according to claim 1, wherein the isolated component is the phytochrome. 10

7. The use according to claim 1 , wherein the mixture of isolated components consist of mycosporine-like amino acids, phycocyanin, phycoerithrocyanin and phytochrome.

8. The use according to claim 8, wherein said mixture additionally contains . phenylethylamine (PEA). 15

9. The use according to claim 1 , wherein said composition is suitable for human administration.

10. The use according to claim 1 , wherein the AFA Klamath preparation, the extract or the isolated component thereof is formulated with pharmaceutically acceptable vehicles or excipients. 20

11. The use of an isolated component of the microalga Aphanizomenon Flos Aquae Aquae Ralfs ex Born. & Flah. Var: flos aquae (AFA Klamath} which is selected from AFA-phycocyanin (AFA-PC) and the chromophore phycocyanobilin AMENDED SHEET -0.4-2008 . EP2007005622 - 40 - (PCB) for the preparation of a neuroprotective agent.

12. A method for inhibiting the enzyme monoaminoxtdase B in a subject in need thereof, which comprises administering to said subject an isolated AFA Klamath component selected from phytochrome, phycocyanin, 5 phycoerithrocyanin and mycosporine-like amino acids or mixtures thereof.

13. A method according to claim 1 1 , wherein said subject is a human subject affected by a catechofamine-associated neurological or neurodegenerative disease. For the Applicants REINHOLO COHN AND PARTNERS By: AMENDED SHEET